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Supply of Prodigy Glucose Control Solution Low Level 1

Active

Federal

Response Deadline10/28/2026, 05:00:00 PM UTC

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

AI Contract Overview

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This subcontract involves the supply of Prodigy Glucose Control Solution Low Level 1 for in vitro diagnostic use to support prime contractors on Department of Defense supply contracts. Managed by the Medical Supply Chain MD Surg FSF, the agreement requires the delivery of two units FOB Destination to Fort Bragg. The contractor must ensure all products comply with FDA regulations, Medical Marking Standard No. 1, RA001 technical requirements, and RP001 packaging standards. Additionally, the supplied solutions must have a non-extendable shelf life of 24 months upon delivery.

General Info

Supply two FDA-compliant Prodigy Glucose Control solutions to Fort Bragg for DoD contracts.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

NAICS

423450 - Medical, Dental, and Hospital Equipment and Supplies Merchant Wholesalers

Place of Performance

FORT BRAGG, NC, 28310, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-27-T-0855.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

CONTROL, GLUCOSE

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Timeline

PostedOct 22

subcontract

Response DeadlineOct 28

Submission deadline

Response Deadline

10/28/2026, 05:00:00 PM UTCin 6 days

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

ContactsNo contacts available

OfficeN/A

Organization / AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

Office AddressN/A

ContactsNo contact information available

Full Description

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Supplies medical diagnostic control solution for prime contractors on DLA supply contracts. Provides Prodigy Glucose Control Solution Low Level 1 (NSN 6550-01-686-4885) for in vitro diagnostic use. Ensures compliance with Medical Marking Standard No. 1, RA001 technical requirements, and RP001 packaging standards. Requires FDA regulation compliance and a non-extendable 24-month shelf life upon delivery. Delivers 2 units FOB Destination.

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